The primary remit of the TRISARC is to review large amounts of medical (mainly safety) data flowing through the clinical trial environment in order to ensure patient data is complete and medically accurate
Job Summary
The primary remit of the TRISARC is to review large amounts of medical (mainly safety) data flowing through the clinical trial environment in order to ensure patient data is complete and medically accurate.
The Analyst, Clinical Trial Safety is responsible for support of tools set-up & maintenance, scripting, data analysis tasks for the Clinical Trial Safety.
AstraZeneca prides itself on crafting a collaborative culture that champions knowledge-sharing, ambitious thinking and innovation.
Matching Summary
The primary remit of the TRISARC is to review large amounts of medical (mainly safety) data flowing through the clinical trial environment in order to ensure patient data is complete and medically accurate.